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February 28, 2013 is Rare Disease Day. Part of the Multiple System Atrophy Coalition’s new mission statement is to advocate for MSA awareness. As such, Don Crouse, an MSA Coalition Board member will be heading to Washington, DC next week to participate in Rare Disease Day advocacy activities, including meetings with various Senators and U.S. representatives to discuss the need for greater research funding for rare diseases. The MSA Coalition will be joined by more than 200 other individuals representing many other rare diseases.